HCID 57847118, compound → HCID 57846922, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][C:3]([C@H:6]2[C@H:15]3[CH2:16][CH2:17][N:18]([C:19]([C@H:21]4[CH2:26][CH2:25][CH2:24][CH2:23][C@H:22]4[NH:27][C:28](=[O:35])[C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)=[O:20])[C@H:14]3[C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[NH:7]2)=[CH:2]1.S1C=CC([C@H]2[C@@H]3CCN(C([C@H]4CCCC[C@H]4NC(=O)C4C=CC=CC=4)=O)[C@@H]3C3C=CC=CC=3N2)=C1>C1(C)C=CC=CC=1.[O-2].[O-2].[Mn+4]>[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[C:15]3[CH2:16][CH2:17][N:18]([C:19]([C@H:21]4[CH2:26][CH2:25][CH2:24][CH2:23][C@H:22]4[NH:27][C:28](=[O:35])[C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)=[O:20])[C:14]=3[C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[N:7]=2)=[CH:2]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of N-((1R,2S)-2-{[(3aR*,4R*,9bR*)-4-(3-thienyl)-2,3,3a, 4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexyl)benzamide and N-((1R,2S)-2-{[(3aS*,4R*,9bS*)-4-(3-thienyl)-2,3,3a, 4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexyl)benzamide (422 mg, 0.87 mmol) was dissolved in toluene (30 ml), manganese dioxide (7.6 g, 87 mmol) was added and the mixture was refluxed overnight. The reaction mixture was filtered through celite and washed with methanol. The filtrate was concentrated under reduced pressure. The residue was subjected to column chromatography using silica gel (30 g), and eluted with hexane-ethyl acetate (9:1-2:1, v/v). Crystallization from diisopropy ether gave the title compound (70 mg, 17%) as pale-brown crystals.
Workup
- temperaturethe mixture was refluxed overnight
- filtrationThe reaction mixture was filtered through celite
- washwashed with methanol
- concentrationThe filtrate was concentrated under reduced pressure
- washeluted with hexane-ethyl acetate (9:1-2:1
- customCrystallization from diisopropy ether
Sources & evidence
- ORD record
- ord-cb72ae8b2950490ba5342d26231b7aa9
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07592453B2
Reaction notes
Loading…